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FDA 510(k)

LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73

K-Number: K883615 · 1988-12-16

ApplicantSupelco, Inc.
Decision Date1988-12-16
Product CodeDJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1988-12-16 under 510(k) number K883615. The device is classified under product code DJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73?

LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 is a medical device that received FDA 510(k) clearance on 1988-12-16. The listed applicant is Supelco, Inc.. The 510(k) number is K883615.

When did LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 receive FDA 510(k) clearance?

LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 received FDA 510(k) clearance on 1988-12-16, under 510(k) number K883615.

Who is the listed applicant for LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73?

The FDA 510(k) record lists Supelco, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73?

The FDA product code for LIQUID CHROMATOGRAPHY COLUMNS 5-7070/71/72/73 is DJY.

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Other records listing Supelco, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K894141LIQUID CHROMATOGRAPHY COLUMNSK884403LIQUID CHROMATOGRAPHY COLUMNS SOLID PHASE EX. TUBEK881868LIQUID CHROMATOGRAPHY COLUMNS HISEP COLUMN & GUARDK881361SOLID PHASE EXTRACTION TUBESK880724LIQUID CHROMATO. COLUMNSK874824CAPILLARY COLUMNS FOR GAS CHROMATOGRAPHY

View all 24 devices →

Related Devices (Code: DJY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K890113THE CDI(R) SYSTEM 400Cardiovascular Devices, Inc.K881361SOLID PHASE EXTRACTION TUBESSupelco, Inc.K850963DUPONT PREP TYPE SI EXTRACITON CARTRIDGEE.I. Dupont DE Nemours & Co., Inc.K840985TRISACRYL GF 05 & TRISACRYL GF 2000Lkb Instruments, Inc.K832198HC40/HC75 PREPACKED COLUMSHamilton Co.K831289PREFILLED IEC COLUMNSBerwick Medical Products, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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